Drug Facts
Active Ingredient. Purpose
Benzalkonium Chloride 0.1%...........Antimicrobial
Afia Alcohol-free Foaming Hand Sanitizer
FDA Label NDC 71023-445
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by National Chemical Laboratories, Inc. for the product Afia Alcohol-free Foaming Hand Sanitizer (NDC 71023-445). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, uses, warnings:, directions, inactive ingredients, otc - keep out of reach of children, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
- For hand sanitizing to decrease bacteria on the skin
- Recommended for repeated use
For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use
Warnings:
For external use only.
When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.
Stop use and ask doctor if irritation or redness developts, or if condition persists for more than 72 hours.
Directions
- Pump a small amount of foam into palm of hand
- Rub thoroughly over all surfaces of both hands
- Rub hands together briskly until dry
Inactive Ingredients
Water, dihyroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Package Label.Principal Display Panel
Afia Alcohol-Free Foaming Hand Sanitizer
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